Home › Companies › Careers Rocketpharma Icims Com › Specialist, Quality Document Control
Specialist, Quality Document Control
Careers Rocketpharma Icims Com · Cranbury, NJ, US · On Site · Active · $56,000–$68,000 / year · iCIMS
Job facts
| Field | Value |
|---|---|
| Company | Careers Rocketpharma Icims Com |
| Title | Specialist, Quality Document Control |
| Normalized title | - |
| Department / team | Quality Assurance |
| Location | Cranbury, NJ, United States |
| Work model | On Site |
| Employment type | Full Time |
| Salary | $56,000–$68,000 / year |
| Status | active |
| ATS provider | iCIMS |
| Posted / first seen | 2026-04-10 / 2026-05-31 |
| Changed / last seen | 2026-06-01 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Careers Rocketpharma Icims Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through iCIMS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Cranbury. | Open |
| Department jobs | Active postings in Quality Assurance. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Careers Rocketpharma Icims Com |
| Source | 8f622a14-eebd-483c-84e3-f2ef0672afd5 |
| ATS provider | iCIMS |
Description
Overview
Create a future where DNA is no longer destiny. Join Rocket Pharma.
Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We are a team of creative, compassionate, and driven individuals united by a profound mission of seeking gene therapy cures. Rocket places tremendous value on our people and fosters a collaborative environment where bold ideas thrive and every team member makes a meaningful impact. Our core values guide everything we do: we trust one another, show generosity toward patients, embrace curiosity, and strive to elevate science. Team members receive a competitive total rewards package, including equity participation, 401(k) matching, and excellent health benefits.
Position Summary
The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system. This role will manage all paper-based documents and records and will be the primary owner of the document control storage room that houses all paper records/logbooks, batch records, etc.
Responsibilities
Management of documents within the ZenQMS electronic quality system.
Issuance and archiving of all paper-based documents and records, including batch records, logbooks, controlled forms, etc.
Oversight and management of the on-site physical document storage room
Support the various functional groups in managing their documents
Supporting the ZenQMS team in managing documents within the system
Qualifications
Associates Degree - Degree in science related field preferred
Minimum three years of experience in a document control or document management role
Experience with electronic document management systems (ZenQMS, Veeva, etc.)
Minimum of 3-5 years of quality biopharma experience
Familiar with standard software systems (Microsoft Word, Excel, PowerPoint, etc.)
Ability to work within a multifunctional team
Work with documents, pushing carts to transport batch records and large sets of documents/binders
Compensation
The expected salary range for this position is $56,000 to $68,000.
At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee’s experience, location of the position and availability of similar talent in a competitive market.
For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts.
In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year’s, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives).
EEO Statement
A diverse workforce fosters innovation and strengthens Rocket’s business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws.
Full job record
| Job ID | 1d5cf11da33c2fbc290ce3d809281977ce9f56cd |
| Org ID | 9d2b7a1a-62cd-42b3-906a-0d84c2de80e1 |
| Source ID | 8f622a14-eebd-483c-84e3-f2ef0672afd5 |
| Board ID | 8f622a14-eebd-483c-84e3-f2ef0672afd5 |
| Provider | icims |
| Provider Job Key | 2129 |
| Title | Specialist, Quality Document Control |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Cranbury, NJ, US |
| Department | Quality Assurance |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | NJ |
| City | Cranbury |
| Salary Raw | Overview Create a future where DNA is no longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We are a team of creative, compassionate, and driven individuals united by a profound mission of seeking gene therapy cures. Rocket places tremendous value on our people and fosters a collaborative environment where bold ideas thrive and every team member makes a meaningful impact. Our core values guide everything we do: we trust one another, show generosity toward patients, embrace curiosity, and strive to elevate science. Team members receive a competitive total rewards package, including equity participation, 401(k) matching, and excellent health benefits. Position Summary The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system. This role will manage all paper-based documents and records and will be the primary owner of the document control storage room that houses all paper records/logbooks, batch records, etc. Responsibilities Management of documents within the ZenQMS electronic quality system. Issuance and archiving of all paper-based documents and records, including batch records, logbooks, controlled forms, etc. Oversight and management of the on-site physical document storage room Support the various functional groups in managing their documents Supporting the ZenQMS team in managing documents within the system Qualifications Associates Degree - Degree in science related field preferred Minimum three years of experience in a document control or document management role Experience with electronic document management systems (ZenQMS, Veeva, etc.) Minimum of 3-5 years of quality biopharma experience Familiar with standard software systems (Microsoft Word, Excel, PowerPoint, etc.) Ability to work within a multifunctional team Work with documents, pushing carts to transport batch records and large sets of documents/binders Compensation The expected salary range for this position is $56,000 to $68,000. At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee’s experience, location of the position and availability of similar talent in a competitive market. For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts. In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year’s, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives). EEO Statement A diverse workforce fosters innovation and strengthens Rocket’s business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws. |
| Salary Min | 56,000 |
| Salary Max | 68,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://careers-rocketpharma.icims.com/jobs/2129/specialist%2c-quality-document-control/job |
| Apply URL | https://careers-rocketpharma.icims.com/jobs/2129/specialist%2c-quality-document-control/job |
| First Seen At | 2026-05-31 18:43:28Z |
| Last Seen At | 2026-06-06 08:29:08Z |
| Last Checked At | 2026-06-06 08:29:08Z |
| Last Changed At | 2026-06-01 13:59:05Z |
| Inactive At | — |
| Source Posted At | 2026-04-10 04:00:00Z |
| Source Updated At | 2026-04-14 14:07:46Z |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=icims/board=careers-rocketpharma.icims.com/date=2026-06-06/2026-06-06T08-29-08-181Z-d1da8c0fa62cfc7841abd5e88cab0cea9baea1d57e664a093803eba401072fc4.json |
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